Derivatives of 1-amino-7-naphthol.



QED. STATES PATENT oFrroE.

mm. JULIUS AND-ERNST russnnneenn, or LUIDWIGSHAFEN-ON-THE-RHiINE,-A1\fD ,LOUISBLANGEY, F MANNHEIM, GERMANY, ASSIGNORS 'IO BADISCHE ANILINfic SODA. FABRIK, OF LUDWIGSHAFEN-YON'THETRHINE, GERMANY, A. (JOIEtIP0IEtA'l.IIQQH.

DERIVATIVES or i-AMINO-f-NAPHTHQL.

No Drawing.

To all whom it man concern 4 Be it known that we, PAUL JULI Us and. ERNST 'FUssnNEeGER, citizensof the Austro- Hlmgarian Empire, residing at Ludwigshafen-on-the-Rhine, Germany, and LOUIS .BLANGEY, citizen of the Swiss Empire, re-

siding at Mannheim 'Ge'rniany, have inventednew and useful Improvements in De. rivatives of l-Amino-7-Naphthol, of which the 'following is a specification. We have discovered new compound which are derivatives of 1 amino-7 -naphtl1ol and which possess a constitution corresponding to the formula A 5 m n-R in which X represents an oxygen-contain ing group consisting of morethanone, and

. less than four, atoms, which ,may be referred to as a simple divalent acidyl group containing oxygen and R represents a hal- I ogenated benzene resid'ue which contains no other substituent---besides halogen.

Our new compounds can be obtained by causing ahalogenated aromatic acid chlor1d, or a halogenated sulfonyl-chlorid, to. react on 1-amin0-7-naphthol, and they consist when pure of colorless crystalline compounds Which are very diflicultly soluble in water, but are soluble in caustic soda solu- 35 tion and which combine with diazotized ortho-nitranilin giving reddish coloring matters. 1 Coloring matters obtained by -the' use of our new products are claimed 1n a separate application Serial No. 849,873 of even date.

trate further the nature of this invention,

which, however, .is-not. confined to this ex temperature, allow 17 5 parts of ortho-chlorbenzoyl-chlorid to run into the suspension. Gontinue stirring for'twelve hours, then The-following example will serve to illus- I I Specification of Letters Patent. Patented June 27, 1916, Application filed July 9, 914. Serial No. 849,872. r

i add an aqueous solution of 53 parts of cal I cined'soda and distil off the chlorbenzene by filter this solution if necessary, and then,

after cooling, add excess of dilute hydrodesired, the condensation can be carried out 1n the presence of sodium acetate, or of other compound capableof fixing hydro chloric acid. A similar process can be fol- 'means of steam." Treat the residue with 200 parts of 35 per cent. caustlc soda solution, 'whereupon the product goes .into solution,

lowed if ortho-chlor-benzoyl-chlorid be replaced by other halogenated derivatives of benZoyl-chlorid, orv by halogenated deriva# tives of benzene-sulfo-chlorid, such as, for instance para-chlor-benzoyl-chlorid, QA-dichlor-benzoyl-chlorid, or 2.6-dichlor-ben- 'zoyl-chlorid, or para-dichlor-benzene-sulfonyl-chlorid,for' 2.5-dichlor-benzene-sulfonylchlorid.

The following table gives the melting points of some of the products of our invention.

Product j om l-amino-fl-naphtlipl Melting point.

p-Chlorben'zoyl chlorid 230-231 C. 2.-Dichlorbenzoyl-chlorid 182-183 C. 2.6-Dichlorbenzoy1-chlorid; 230-232 C. p-Chlorbenzene-sfilfonyl-chlorid 213214 C. 2.5-Dichlorbenzene-sulfonyl-chlorid 185488 C.

N ow'what we claim isza- I I 1. The new derivatives of 1-am1no-7-naphthol possessing a constitution corresponding to the formula in which X represents a divalent acidyl group containing oigvgen and R is a hal ogenated benzene residue, which new derivatives consist when pure of colorless "crys talline powders, are very diflicultly soluble in water, but are soluble in caustic soda solution and combine with diazotized orthonitranilin giving reddish coloring matters.

2. The new derivatives of l-amino-T-naphthol, which possess a constitution corresponding to the formula in which R represents a halogenated hen zene residue, which new (lGIlYfltlYQS consist, when pure of colorless crystalline powmemes which consists when pure of a colorless crystalline powder, melting at about 157-158 (1., is very diiiicultly soluble in water, but is soluble in caustic alkali solution and combines with diazotized ortho-,-nii;rani lin yielding a Turkey red compound.

In testimony whereof we have hereunto set our hands in the presence of (we suhscribing witnesses.

PAUL JULIUS.

ERKST FUSSEXEGGER. LGUIS BLAXC-TEY.

Ac. LLOYD7 3.1mm: Coclirnsm. 

